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1H-Benzimidazole, 2-butyl-1-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

133052-87-6

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133052-87-6 Usage

Molecular structure

1H-Benzimidazole, 2-butyl-1-[[2'-(1H-tetrazol-5-yl)[1,1'-biphenyl]-4-yl]methyl]consists of a benzimidazole ring fused with a butyl group and a biphenyl-tetrazole moiety.

Biological activity

The presence of tetrazole and benzimidazole moieties suggests potential pharmacological properties and biological activity.

Potential applications

The compound may be used in the development of pharmaceutical drugs or other bioactive compounds.

Interaction with biological targets

The structure of the compound indicates possible interactions with receptors or enzymes in biological systems.

Further research needed

Additional research and testing are required to determine the specific properties and potential applications of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 133052-87-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,0,5 and 2 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 133052-87:
(8*1)+(7*3)+(6*3)+(5*0)+(4*5)+(3*2)+(2*8)+(1*7)=96
96 % 10 = 6
So 133052-87-6 is a valid CAS Registry Number.

133052-87-6Downstream Products

133052-87-6Relevant academic research and scientific papers

New nonpeptide angiotensin II receptor antagonists. 1. Synthesis, biological properties, and structure-activity relationships of 2-alkyl benzimidazole derivatives

Thomas,Allott,Gibson,Major,Masek,Oldham,Ratcliffe,Roberts,Russell,Thomason

, p. 877 - 885 (1992)

On the basis of an extension of the literature lead 1, a series of benzimidazoles have been synthesized and shown to be angiotensin II (AII) receptor antagonists. The structure-activity relationships of these new antagonists have been explored and the key

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